Quality Auditor
Confirmed on the employer's own hiring board on Oct 24, 2026. First seen by Alion on Apr 30, 2026. Abbott scores A on the Alion truth index.
JOB DESCRIPTION:
Within Abbott’s Established Pharmaceuticals Division (EPD), we provide high-quality, trusted medicines that improve access to healthcare around the world.
The Opportunity
Abbott is seeking a Quality Auditor to support supplier and third-party manufacturer oversight for EPD. Based in Weesp, this role plays a critical part in ensuring compliance, quality, and regulatory adherence across Abbott’s external partner network.
You will manage on-site audits and quality assessments for a broad range of suppliers and third-party manufacturers, working closely with internal stakeholders and external partners to drive continuous improvement and ensure patient safety.
What You’ll Do
Plan, prepare, conduct, report, and close on-site audits for suppliers and third-party manufacturers supporting EPD.
Manage Quality Questionnaires for suppliers and third-party manufacturers and resolve any identified issues.
Assess, track, and follow up on Corrective and Preventive Actions (CAPAs) to ensure timely and effective closure.
Ensure all audit activities and outcomes are accurately documented in the Audit Tracking system.
Provide timely audit updates to management and stakeholders, escalating critical findings in line with policies and procedures.
Monitor regulatory developments, standards, and industry trends and integrate them into audit activities.
Support EPD manufacturing sites in resolving supplier-related quality and compliance issues.
Act as the primary quality contact for external partners on auditing matters and promote a proactive quality mindset.
What You’ll Bring
Bachelor’s degree in a relevant scientific or technical discipline (e.g. Chemistry, Pharmacy, Biology, Microbiology, Engineering) or equivalent industry experience.
At least 8 years’ experience in the pharmaceutical, healthcare, or regulatory environment, including a minimum of 3 years of auditing experience (GMP, GDP, ISO).
Strong knowledge of ICH guidelines, GMP standards, WHO guidance, and applicable regional and local regulations.
Proven experience auditing suppliers and/or third-party manufacturers across pharmaceutical, medical device, or nutrition product types.
Strong analytical skills with the ability to identify compliance risks and drive effective corrective actions.
Excellent communication skills with advanced written and verbal Business English.
Fluency in Dutch is required, with the ability to communicate professionally with local stakeholders in the Netherlands.
High level of integrity, independence, adaptability, and cultural awareness, with willingness and ability to travel internationally.
Working at Abbott
At Abbott, you can do work that matters, grow and learn, care for yourself and your family, be your true self, and live a full life. You will have access to career development opportunities within an international company recognized as a great place to work in multiple countries. Abbott has been named one of the most admired companies in the world by Fortune and is recognized for its commitment to diversity, inclusion, and innovation.
We are an equal opportunity employer and value diversity in our workforce. We welcome applications from all qualified individuals regardless of gender, age, ethnicity, religion, disability, sexual orientation, or any other characteristic protected by law.
Recruitment Process
We are conducting recruitment on an ongoing basis and will close the process as soon as the right candidate is found.
If you meet the qualifications and are interested in this opportunity, we encourage you to apply as soon as possible.
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.